Photochemical degradation of acrolein using VUV excimer lamp in air at atmospheric pressure
The photochemical degradation of acrolein (C 2 H 3 CHO) was investigated in air at atmospheric pressure using a 172-nm Xe 2 excimer lamp. When C 2 H 3 CHO was decomposed using the side-on type of lamp, HCOOH, CO, CO 2 , and O 3 peaks were observed in FTIR absorption spectra. The dependence of produc...
Saved in:
Published in | International journal of environmental science and technology (Tehran) Vol. 16; no. 11; pp. 7229 - 7240 |
---|---|
Main Authors | , , , , , , |
Format | Journal Article |
Language | English |
Published |
Berlin/Heidelberg
Springer Berlin Heidelberg
01.11.2019
|
Subjects | |
Online Access | Get full text |
Cover
Loading…
Summary: | The photochemical degradation of acrolein (C
2
H
3
CHO) was investigated in air at atmospheric pressure using a 172-nm Xe
2
excimer lamp. When C
2
H
3
CHO was decomposed using the side-on type of lamp, HCOOH, CO, CO
2
, and O
3
peaks were observed in FTIR absorption spectra. The dependence of product concentrations on the irradiation time indicated that HCOOH and CO intermediates are finally converted to CO
2
via consecutive reactions. The degradation rate coefficient of C
2
H
3
CHO in the batch system increased from 8.4 to 19.3 min
−1
, as the O
2
concentration was decreased from 20 to 1%. It increased also from 8.4 to 40.1 min
−1
at 20% O
2
, as the chamber depth was decreased from 3.0 to 0.5 cm. The best energy efficiency of the C
2
H
3
CHO degradation was 3.4 g kW
−1
h
−1
at 1–20% O
2
in a flow system. Besides direct VUV photodissociation of C
2
H
3
CHO, reactions of O(
3
P,
1
D) and O
3
, produced from photolysis of O
2
, can contribute to C
2
H
3
CHO degradation in the initial stage. Among them, the contribution of O(
1
D) and O
3
was found to be insignificant on the basis of the total pressure dependence of removal amount of C
2
H
3
CHO and results obtained from the O
3
+ C
2
H
3
CHO reaction. It was concluded that at first C
2
H
3
CHO is decomposed by direct VUV photodissociation of C
2
H
3
CHO and the O(
3
P) + C
2
H
3
CHO reaction. It was further decomposed by secondary reactions of O(
3
P), OH, and O
3
with such intermediates as HCOOH and CO and finally oxidized to CO
2
. |
---|---|
ISSN: | 1735-1472 1735-2630 |
DOI: | 10.1007/s13762-019-02404-5 |